Monografie
Mechanisms and modifiers of energy metabolism in ALS and Huntington disease
- Sprache
-
Englisch
- Anmerkungen
-
Ulm, Universität Ulm, Habil.-Schr., 2016
- Identifier
-
1088553192
Thema
Myatrophische Lateralsklerose; Mitochondrium; Huntington-Chorea; Nervendegeneration; Hirnkrankheit; Neuropsychiatrie; Nervenkrankheit; Hochschulschrift
Beteiligte Personen und Organisationen
Weydt, Patrick
- URN
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
26.01.2023, 13:56 MEZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Objekttyp
- Monografie
Beteiligte
- Weydt, Patrick
Ähnliche Objekte (12)
G3 Hedonic olfaction in huntington’s disease
Error processing in Huntington's disease
Nucleolar stress controls mutant Huntington toxicity and monitors Huntington’s disease progression
Behavioral neurobiology of Huntington's disease and Parkinson's disease
Tracking disease progression in Huntington’s Disease using electrophysiology of the sensorimotor system
Epigenomic Remodeling in Huntington’s Disease—Master or Servant?
The role of microglia dysfunction in Huntington’s Disease
Working memory-related effective connectivity in Huntington’s disease patients
M4 Safety and tolerability of BN82451B in huntington’s disease
The MID1 protein: a promising therapeutic target in Huntington’s disease
Cortical neurodevelopment in pre-manifest Huntington's disease
Molecular mechanisms in yeast carbon metabolism
G3 Hedonic olfaction in huntington’s disease
Error processing in Huntington's disease
Nucleolar stress controls mutant Huntington toxicity and monitors Huntington’s disease progression
Behavioral neurobiology of Huntington's disease and Parkinson's disease
Tracking disease progression in Huntington’s Disease using electrophysiology of the sensorimotor system
Epigenomic Remodeling in Huntington’s Disease—Master or Servant?
The role of microglia dysfunction in Huntington’s Disease
Working memory-related effective connectivity in Huntington’s disease patients
M4 Safety and tolerability of BN82451B in huntington’s disease
The MID1 protein: a promising therapeutic target in Huntington’s disease
Cortical neurodevelopment in pre-manifest Huntington's disease
Molecular mechanisms in yeast carbon metabolism
G3 Hedonic olfaction in huntington’s disease
Error processing in Huntington's disease
Nucleolar stress controls mutant Huntington toxicity and monitors Huntington’s disease progression
Behavioral neurobiology of Huntington's disease and Parkinson's disease
Tracking disease progression in Huntington’s Disease using electrophysiology of the sensorimotor system
Epigenomic Remodeling in Huntington’s Disease—Master or Servant?
The role of microglia dysfunction in Huntington’s Disease
Working memory-related effective connectivity in Huntington’s disease patients
M4 Safety and tolerability of BN82451B in huntington’s disease
The MID1 protein: a promising therapeutic target in Huntington’s disease
Cortical neurodevelopment in pre-manifest Huntington's disease